| Multiple phenotypes in phosphoglucomutase 1 deficiency LC Tegtmeyer, S Rust, M van Scherpenzeel, BG Ng, ME Losfeld, S Timal, ... New England Journal of Medicine 370 (6), 533-542, 2014 | 287 | 2014 |
| Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation BG Ng, KJ Buckingham, K Raymond, M Kircher, EH Turner, M He, ... The American Journal of Human Genetics 92 (4), 632-636, 2013 | 124 | 2013 |
| The cell surface expressed nucleolin is a glycoprotein that triggers calcium entry into mammalian cells ME Losfeld, D El Khoury, P Mariot, M Carpentier, B Krust, JP Briand, ... Experimental cell research 315 (2), 357-369, 2009 | 95 | 2009 |
| Mutations in STT3A and STT3B cause two congenital disorders of glycosylation S Shrimal, BG Ng, ME Losfeld, R Gilmore, HH Freeze Human molecular genetics 22 (22), 4638-4645, 2013 | 93 | 2013 |
| DDOST mutations identified by whole-exome sequencing are implicated in congenital disorders of glycosylation MA Jones, BG Ng, S Bhide, E Chin, D Rhodenizer, P He, ME Losfeld, ... The American Journal of Human Genetics 90 (2), 363-368, 2012 | 80 | 2012 |
| The Metabolic Origins of Mannose in Glycoproteins*♦ M Ichikawa, DA Scott, ME Losfeld, HH Freeze Journal of Biological Chemistry 289 (10), 6751-6761, 2014 | 77 | 2014 |
| A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex ME Losfeld, BG Ng, M Kircher, KJ Buckingham, EH Turner, A Eroshkin, ... Human molecular genetics 23 (6), 1602-1605, 2014 | 61 | 2014 |
| Identification of intercellular cell adhesion molecule 1 (ICAM-1) as a hypoglycosylation marker in congenital disorders of glycosylation cells P He, BG Ng, ME Losfeld, W Zhu, HH Freeze Journal of Biological Chemistry 287 (22), 18210-18217, 2012 | 48 | 2012 |
| Modulation of HSP70 GlcNAc-directed lectin activity by glucose availability and utilization C Guinez, ME Losfeld, R Cacan, JC Michalski, T Lefebvre Glycobiology 16 (1), 22-28, 2006 | 46 | 2006 |
| Influence of protein/glycan interaction on site‐specific glycan heterogeneity ME Losfeld, E Scibona, CW Lin, TK Villiger, R Gauss, M Morbidelli, ... The FASEB Journal 31 (10), 4623-4635, 2017 | 43 | 2017 |
| Quantitative profiling of N-linked glycosylation machinery in yeast Saccharomyces cerevisiae K Poljak, N Selevsek, E Ngwa, J Grossmann, ME Losfeld, M Aebi Molecular & Cellular Proteomics 17 (1), 18-30, 2018 | 37 | 2018 |
| A sensitive green fluorescent protein biomarker of N-glycosylation site occupancy ME Losfeld, F Soncin, BG Ng, I Singec, HH Freeze The FASEB Journal 26 (10), 4210, 2012 | 36 | 2012 |
| N‐glycosylation influences the structure and self‐association abilities of recombinant nucleolin ME Losfeld, A Leroy, B Coddeville, M Carpentier, J Mazurier, D Legrand The FEBS journal 278 (14), 2552-2564, 2011 | 29 | 2011 |
| Mutations in the translocon‐associated protein complex subunit SSR3 cause a novel congenital disorder of glycosylation BG Ng, CM Lourenço, ME Losfeld, KJ Buckingham, M Kircher, ... Journal of inherited metabolic disease 42 (5), 993-997, 2019 | 21 | 2019 |
| Glycan–protein interactions determine kinetics of N-glycan remodeling C Mathew, RG Weiß, C Giese, C Lin, ME Losfeld, R Glockshuber, ... RSC Chemical Biology 2 (3), 917-931, 2021 | 20 | 2021 |
| N-glycosylation enhances conformational flexibility of protein disulfide isomerase revealed by microsecond molecular dynamics and Markov state modeling RG Weiß, ME Losfeld, M Aebi, S Riniker The Journal of Physical Chemistry B 125 (33), 9467-9479, 2021 | 14 | 2021 |
| University of Washington Center for Mendelian Genomics Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation BG Ng, KJ Buckingham, K Raymond, M Kircher, EH Turner, M He, ... Am. J. Hum. Genet 92, 632-636, 2013 | 10 | 2013 |
| Glycosylation network mapping and site-specific glycan maturation in vivo ME Losfeld, E Scibona, C Lin, M Aebi Iscience 25 (11), 2022 | 5 | 2022 |
| Program and abstracts for the 2012 Joint Meeting of the Society for Glycobiology & American Society for Matrix Biology R Schnaar, JC Paulson, MS Macauley, C Nycholat, F Pfrengle, ... Glycobiology 22 (11), 1518, 2012 | 2 | 2012 |
| Congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex (789.3) ME Losfeld, B Ng, M Kircher, K Buckingham, E Turner, A Eroshkin, ... The FASEB Journal 28, 789.3, 2014 | 1 | 2014 |
